A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390361



Internal ID21047914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:178531303..178639737hg38UCSC Ensembl
chr4:179452457..179560891hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38108435
hg19108435
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212806
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer